Cas no 1170585-19-9 (6-Amino-7-azaindole Dihydrochloride)

6-Amino-7-azaindole dihydrochloride is a heterocyclic organic compound featuring an amino-substituted azaindole core, with two hydrochloride salts enhancing its solubility and stability. This derivative is particularly valuable in medicinal chemistry and pharmaceutical research, serving as a versatile intermediate for the synthesis of biologically active molecules, including kinase inhibitors and other therapeutic agents. Its structural framework allows for efficient functionalization, making it useful in scaffold diversification and drug discovery. The dihydrochloride form ensures improved handling and storage characteristics compared to the free base. High purity grades are typically available to meet rigorous research and industrial application standards.
6-Amino-7-azaindole Dihydrochloride structure
1170585-19-9 structure
Product Name:6-Amino-7-azaindole Dihydrochloride
CAS No:1170585-19-9
MF:C7H9Cl2N3
MW:206.072458982468
MDL:MFCD11035724
CID:1056114
PubChem ID:44118653
Update Time:2025-05-26

6-Amino-7-azaindole Dihydrochloride Chemical and Physical Properties

Names and Identifiers

    • 1H-Pyrrolo[2,3-b]pyridin-6-amine dihydrochloride
    • 6-Amino-7-azaindole Dihydrochloride
    • 6-Amino-1H-pyrrolo[2,3-b]pyridine dihydrochloride
    • DTXSID10656936
    • 1H-Pyrrolo[2,3-b]pyridin-6-amine, hydrochloride (1:2)
    • AMY20405
    • 6-amino-7-azaindole 2hcl
    • 6-Amino-7-azaindole DiHCl
    • AKOS015903759
    • SY005073
    • VWB58519
    • CS-0092061
    • AS-31555
    • 1170585-19-9
    • 1H-Pyrrolo[2,3-b]pyridin-6-aminedihydrochloride
    • 1H-Pyrrolo[2,3-b]pyridin-6-amine--hydrogen chloride (1/2)
    • A893456
    • DB-060955
    • 1H-pyrrolo[2,3-b]pyridin-6-amine;dihydrochloride
    • MFCD11035724
    • MDL: MFCD11035724
    • Inchi: 1S/C7H7N3.2ClH/c8-6-2-1-5-3-4-9-7(5)10-6;;/h1-4H,(H3,8,9,10);2*1H
    • InChI Key: PXZDBOQMBYQRNF-UHFFFAOYSA-N
    • SMILES: Cl.Cl.N1C=CC2=CC=C(N)N=C12

Computed Properties

  • Exact Mass: 205.01700
  • Monoisotopic Mass: 205.0173527g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 0
  • Complexity: 126
  • Covalently-Bonded Unit Count: 3
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 54.7?2

Experimental Properties

  • PSA: 54.70000
  • LogP: 3.33030

6-Amino-7-azaindole Dihydrochloride Security Information

6-Amino-7-azaindole Dihydrochloride Customs Data

  • HS CODE:2933990090
  • Customs Data:

    China Customs Code:

    2933990090

    Overview:

    2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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Additional information on 6-Amino-7-azaindole Dihydrochloride

Recent Advances in the Application of 6-Amino-7-azaindole Dihydrochloride (CAS: 1170585-19-9) in Chemical Biology and Pharmaceutical Research

6-Amino-7-azaindole dihydrochloride (CAS: 1170585-19-9) has emerged as a pivotal scaffold in medicinal chemistry and chemical biology due to its unique structural properties and versatile pharmacological applications. Recent studies have highlighted its role as a privileged heterocyclic motif, particularly in the development of kinase inhibitors and other targeted therapies. This research briefing synthesizes the latest findings on this compound, focusing on its synthesis, biological activity, and potential therapeutic applications.

One of the most significant breakthroughs involves the optimization of synthetic routes for 6-Amino-7-azaindole dihydrochloride, enabling higher yields and improved purity. Researchers have developed novel catalytic methods that reduce byproduct formation, which is critical for scaling up production for preclinical and clinical studies. These advancements are documented in recent publications in journals such as the Journal of Medicinal Chemistry and Bioorganic & Medicinal Chemistry Letters.

In terms of biological activity, 6-Amino-7-azaindole dihydrochloride has shown promising results as a core structure in kinase inhibitors. Specifically, it has been utilized in the design of compounds targeting protein kinases involved in cancer and inflammatory diseases. Recent in vitro and in vivo studies demonstrate its efficacy in modulating kinase activity with high selectivity, reducing off-target effects. These findings are supported by crystallographic data revealing the binding modes of derivatives within kinase active sites.

Furthermore, the compound's potential extends beyond oncology. Recent preclinical studies have explored its application in neurodegenerative diseases, where it acts as a modulator of key signaling pathways implicated in neuroprotection. Researchers have also investigated its role in infectious diseases, particularly in the inhibition of viral polymerases. These diverse applications underscore the compound's versatility and its growing importance in drug discovery pipelines.

Looking ahead, the integration of computational chemistry and machine learning approaches is expected to accelerate the discovery of new 6-Amino-7-azaindole dihydrochloride derivatives with enhanced pharmacological profiles. Collaborative efforts between academia and industry are also paving the way for the translation of these findings into clinical candidates. This briefing concludes with a discussion of ongoing clinical trials and future research directions, emphasizing the compound's potential to address unmet medical needs across multiple therapeutic areas.

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